A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420095



Internal ID21077648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38265201..38270900hg38UCSC Ensembl
chr8:38122719..38128418hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226466
Samples
Known GenesPPAPDC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420095
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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